Regenerable adsorption unit

ABSTRACT

An adsorption unit comprising an adsorbent hollow fibre in which the fibre includes an active component and means for transmitting heat.

The present invention is directed towards the preparation and use ofregenerable adsorption units and in particular regenerable hollow fibresand electrically regenerable fibres.

The range of regenerable adsorption units provided by the presentinvention may be very useful to many process industries. The developmentof rapid thermal swing, electrically regenerable adsorption units is animportant element of the introduction of new energy saving andenvironmentally friendly technologies all over the world. For example,such technology is applicable for valuable material recovery andrecycling, pollution control, gas separation, drying, wastewatertreatment, and recovery of material from waste gases. There is anincreasing need for removal and recovery of noxious species such ascarbon dioxide and other volatile organic compounds (VOCs) from gasand/or liquid streams. The adsorbed compound may then be desorbedelectrically and optionally be recycled (if appropriate) or removed fordownstream processing and safe disposal. The method for removing suchcompounds must have a low capital and operational cost and a lowenvironmental impact.

The desorption of adsorbates after they have been used to adsorb intothe matrix of the fibre the selected components can be achieved in anumber of ways (temperature, vacuum and depressurisation) but the mostcommon is by the application of temperature. Current techniques formaintaining the adsorption properties of a unit generally involve theremoval of the adsorbent from the unit where the adsorption occurs andheating this to regenerate it. This may be done, for example, in an ovenpassing a heated gas stream through the adsorbent bed or using planarheaters. This is expensive in both time (generally requires a minimum of24 hours at the elevated temperature) and capital and operational cost.Having to shut the system down while the adsorbent is removed from theunit for treatment is inefficient Alternatively, having a twin bedsystem where one adsorbent bed does the adsorption while the otherundergoes regeneration increases the inventories and the unit will belarger and substantially less economical.

External ovens have a high capital and operational cost, uneventemperature distribution in the bed and also take time to heat theadsorbent materials (as well as the surrounding air) to the necessarytemperature and to cool down to ambient or operating temperatures again.In some cases, it may not currently be economically viable to regeneratethe adsorbent and the used material is simply removed and replaced witha new unit.

There is therefore a need for an efficient and cost effectiveregenerable adsorption unit.

According to the present invention there is provided an adsorption unitcomprising a hollow fibre in which the fibre includes an activecomponent and means for transmitting heat. The active component isselected to be highly sensitive and reactive to the component orcomponents of choice and desorbs the selected component or components ata reasonable temperature and under low or no vacuum or a combination ofthe two. The active component in the unit will adsorb the selectedcomponent or components while the unit is in use. When the activitydrops below a pre-determined level or after a predetermined number ofcycles, the unit is regenerated. This may be e by the direct applicationof heat to the active adsorbent in the unit.

Adsorbent hollow fibres may advantageously be used as adsorption unitsas they have a high surface area to volume ratio for the adsorption totake place on, can be flexible, have a low pressure drop for energyefficiency, have a superior kinetic adoption preference compared toexisting units, and have a resistance to adsorption (prevent down streamequivalent and valves blocking). In particular a bundle of adsorbenthollow fibres may be used through which the fluid may pass. Themolecules to be separated may be adsorbed onto the walls by Van derWaals forces and/or by molecular sieving.

The adsorbent, for example zeolites (in particular high silica zeolites)with a range of pore sizes can simultaneously operate as a molecularsieve and adsorb the selected component. There is then a carbon mixedactive layer which carries the current for heating the fibre.Alternatively, the carbon fibre could act as an adsorbent as well asproviding the heating medium although this is less preferred. In anotheralternative, semi-conducting powder in a layer may act as the heatingmedium.

The heat may be applied by any suitable means. In one embodiment of theinvention, the means for transmitting heat is an electrically conductivecomponent and the heating comprises the application of a voltage betweenthe two ends of the fibre. The passing of an electrical current throughthe fibre by means of the conductive component results in localisedheating which thereby desorbs the active component. The application ofthe voltage heats the active component more quickly than if they wereplaced in an oven and the active component cools more quickly than if ithad been heated in an oven on the removal of the electric current. Thetime taken for the desorption is also substantially reduced incomparison to existing techniques as the adsorbent does not have to beremoved from the unit, taken to a heat source (e.g. oven), heated fordesorption, cooled to operating temperatures again and fitted back intothe unit before adsorption can begin again. The regeneration may also beassisted by the counter current passing of an inert gas, for exampleheated nitrogen, through the bed as a purge.

In another embodiment, the conductive component is a thermallyconductive material and the heating of the unit comprises the localisedapplication of a heat source, for example by induction. Again, thelocalised application of the hear close to the active material ensuresthat the desorption is conducted more quickly than when using heating intraditional packed beds. The active material is heated up and cooledmore quickly than in traditional means.

The hollow fibre may comprise one or more layer. The layers may all havethe same composition or they may have different compositions. Theconductive material may be in each layer or it may only be in one layer,preferably the outer layer. The hollow fibre must be sufficiently porousfor the gaseous material to be adsorbed is able to pass through it suchthat the adsorbent can react with the selected component or components.Therefore the mean pore size in one or more layers (including the outerlayer) may be less than 5 μm. For example, the mean pore size in the oneor more layers may be less than 1 μm or less than 500 nm, or less than100 nm, or less than 10 nm.

The hollow fibre may be organic and comprise a polymer, an additive, anadsorbent material and an electrically conductive material. The polymermay be selected from the group consisting of polysulfone (PSF),polyvinylidenefluoride (PVDF)), polyethylene, polypropylene,poly(phenylene oxide), polyacrylonitrile, polymethylmethacrylate,poly(vinyl chloride), Poly ether sulfone (PESF), Cellulose acetate,Polyamide (aromatic), Polyimide, Poly(ether imide) and poly(vinylalcohol), co-polymers of Polylactide (PLA) and Polyglycolide (PGA),Polycaprolactone (PCL) and Poly(ethylene terephathalate) (PET) or anypolymer that dissolves in the solvents. In preparation, the fibre mayhave a temperature pre-treatment, for example, at about 200° C., toremove any trapped polymer solvents and moisture and to allow access tothe adsorbent particles.

The additive may be present to improve transport properties and may beselected from poly (vinyl alcohol), polyvinyl pyrrolidone (PVP)polyacrylic acid (PAA), calcium chloride and fumed silica.

The adsorbent may be a zeolite, for example a high silica zeolite suchas silicalite and ZSM5, or other molecular sieve materials such asMCM41, MCM48, silica adsorbents or activated carbon powders, or ionexchange resins.

The hollow fibre may be inorganic and comprise an inorganic powder, abinder, an adsorptive component or reactive component and anelectrically conductive component. The inorganic powder may be selectedfrom the group consisting of ceramics, adsorbents and ion exchangeresins. The ceramic may be selected from the group consisting ofaluminium oxide bentonite, silica, hydroxyapatite or mixtures thereofThe binder may be selected from lead bisilicate frit, fine standardborax fit, bentonite and Hyplas. The inorganic fibres are produced byusing a polymer, a binder and an adsorptive or reactive component suchas a zeolite or ion exchange resin. The fibre is fired to burn thepolymer and to partially melt the binder to hold the adsorbent orreactive particles in the structure. The firing temperature should bebelow the melting temperature of the adsorbent to avoid any loss ofactivity, for example at less than 700° C.

The electrically conductive component may be selected from the groupconsisting of silver, metal powder (e.g. copper), carbon, conductingpolymers, conducting cement, semiconductor materials and combinationsthereof. For example, the conducting layer may comprise one or more ofpolyaniline, carbon black, activated charcoal, copper powder,polyaniline composite with 10-30% (for example 15-25% or 20%) carbonblack and silver conductive paste.

The inorganic adsorbent fibre may have a flexibility of greater than 5°bending angle from the mid point of the fibre, preferably greater than10°, 20° or 30°. The bending angle of fibres produced according to thepresent invention was measured by taking a 20 cm length of the inorganicfibre, mounting this on two rods, one at each end, and one of the rodswas moved, downwards at a speed of 2 cm/min until the fibre snapped. Theangle of flex (bending angle) was then measured between the mid point ofthe fibre in the horizontal position to the end point where the fibresnapped.

The inorganic adsorbent hollow fibre may have a mechanical strength(load) of greater than 200 g force at a crosshead speed of 1.0 mm/minfor a sample which has an effective surface porosity of 1000-3000 (ε/q²calculated from Knudsen flow method). Optionally the load at breakingpoint is greater than 250 g force or greater than 300 g force. Apreferred range is 250-800 g, more preferably is 300-700 g force andmost preferred 400-650 g. Increased mechanical strength may be obtainedby producing multiple layer fibres. Particularly preferred are double ortriple or quadruple layer fibres. Double layer fibres are stronger thansingle layer fibres and triple layer fibres are mechanicallysubstantially stronger than double layer fibres.

A further advantage to the production of double or triple or quadruplelayer fibres fin addition to the substantially increased mechanicalstrength) is that the fibres are largely defect free. With two or threelayers of the same composition, any defects in one layer are extremelyunlikely to be mirrored by a similar defect in the next layer. The neteffect is that there are no pin holes in the fibre produced and it cantherefore be used as an efficient porous layer or membrane. This benefitis present for both inorganic adsorbent fibres and for adsorbentpolymeric fibres. It is also possible to produce fibres with a gradedpore structure which may improve the filtration properties.

Further, it is possible to have different compositions in the two ormore layers. It is therefore possible to produce a fibre where eachlayer is tailored towards a particular property. For example, the innerlayer may be of a composition to provide a particular strength to thefibre, but the outer layer may be constructed, to provide the necessaryheat transfer means to enable the adsorbent to be desorbed. Other layersmay have properties to adsorb different components or have aparticularly small pore size for sieving or filtration purposes etc.Each layer could be constructed from powders which are electricallyconducting. This allows the manufacture of a low resistance fibre withlow resistance in each layer and consequently a low voltage requirementfor heating.

The porous hollow fibre optionally has a surface area to volume ratiogreater than 1,000 The area to volume ratio may be in the range1,000-10,000 m²/m³, preferably 1,000-6,000 m²/m³, and most preferably2,000-4,000 m²/m³.

The adsorbent hollow fibre optionally includes a high percentage ofadsorbent material. According to one embodiment, there is at least 65%adsorbent material, preferably at least 75% and more preferably at least80% or 90%. The adsorbent material may be a silicalite, preferably azeolite and more preferably a high silica zeolite, silica, carbon or ionexchange resin. Including a zeolite in the composition restricts theoperating temperature range for the drying and firing (if present)processes. Zeolites lose their functionality if subjected totemperatures of greater than approximately 700-750° C.

The outer diameter of the fibres produced can be 400 μm-2.5 cm dependingon the diameter of the spinneret used to produce the fibres and thenumber of layers used. Therefore, lightweight and compact adsorptionunits or membranes can be made using a single hollow fibre or a clusterof narrower adsorbent fibres as appropriate. The hollow fibres arenanoporous or microporous and can be tailored to exhibit significantadsorption capacity, gas fluxes, bending strength (flexibility) andbursting pressure (7-15 bar). The properties of the fibre can betailored to individual situations.

Flexible hollow fibres are much more resistant to stresses caused duringinstallation, operation and service, and because they can be muchsmaller in diameter and thus the surface area to volume ratio is muchlarger, bundles of such fibres can process a great deal more gas/liquidthan existing tubular membranes or adsorption units (and thus are farmore economical).

If different compositions are used for the different layers, then it maybe possible to have a selective porous layer which can absorb differentcompounds at different rates. It is also possible to have one layerpresent for one property (for example, increased strength) and anotherlayer for another property (for example, selectivity towards aparticular molecule or compound).

The invention may be put into practice in a number of ways and a numberof embodiments are shown here by way of example with reference to thefollowing figures, in which:

FIGS. 1 a and 1 b show triple layer fibres according to the presentinvention;

FIGS. 2 a, 2 b and 2 c show SEMs of the individual layers of the triplelayer fibre shown in FIG. 1;

FIGS. 3 a, 3 b and 3 c show an arrangement of a bundle of triple layerfibres;

FIG. 4 shows the response of triple layer fibres to different voltageinputs;

FIG. 5 shows the heating and cooling cycle of triple layer fibres;

FIG. 6 shows the adsorption performance of the triple layer fibres;

FIG. 7 shows the desorption performance of the triple layer fibres;

FIG. 8 shows a double layer fibre according to the present invention;

FIGS. 9 a and 9 b show SEMs of the individual layers of the double layerfibre shown in FIG. 8;

FIGS. 10 a and 10 b show an arrangement of a bundle of double layerfibres;

FIG. 11 shows the heating curve of a double layer fibre as it reachessteady state;

FIG. 12 shows the steady state heating and cooling cycles of the doublelayer fibres;

FIG. 13 shows the adsorption performance of the double, layer fibres;

FIG. 14 shows the desorption performance of the double layer fibres;

FIG. 15 shows the adsorption performance of a double layer fibre; and

FIG. 16 shows the temperature profiles of double layer fibres forexamples 5 to 10 for a range of applied voltages.

TRIPLE LAYER FIBRES

A polymeric three layer conductive adsorbent hollow fibre was producedin accordance with the details below and tested.

Materials

Adsorbents used to demonstrate and exemplify the invention:

-   -   4A zeolites (particle size 5 μm)    -   13X zeolites (particle size used 5 μm).

Main polymer for the examples:

-   -   Polyethersulfone (PESO (from Ameco Performance, USA) with a        glass transition temperature (Tg) of up to 230° C.-250° C. was        used as a common polymer in all the spinning dopes.

Materials for outer conducting layer:

-   -   Polyaniline (emeraldine base, MW 65,000), (Aldrich, UK),        conductive polymer with the Tg up to 300° C.    -   Carbon black (metal basic, fine powder) (Alfa Aesar, UK).    -   Activated charcoal (<40 micrometer) (Fluka, UK).    -   Copper powder (metal basic, <10 μm) (Alfa Aesar, UK)    -   Polyaniline (emeraldine salt), composite 20 wt % on carbon black        (Aldrich, UK).    -   Silver conducting adhesive paste (Alfa Aesar, UK).    -   Semiconductor materials

Preparation of spinning dopes: First layer dope and second layer dope

The required quantity of organic solvent (NMP) was poured into a 250 mlwide-neck bottle and then the desired quantity of polymer (PESF) wasslowly added. The mixture was stirred on a rotary pump to form thepolymer solution. After the clear polymer solution was formed, arequired amount of adsorbent (4A and 13X) was added into the polymersolution slowly. The mixture was stirred by an IKA® WERKE stirrer at aspeed between 500-1000 rpm for 2-4 days to ensure that the adsorbentpowder was dispersed uniformly in the polymer solution. Finally, themixture was put back on a roller to degas and form the uniform spinningdope.

The spinning dope of conductive layer was prepared from requiredquantity of NMP and the desired quantity of conductive polymer(polyaniline). The mixture was filtered through a 100 μm Nylon filter inorder to remove the non-dissolved polyaniline. The desired quantity ofsecond polymer (PESF) was then added into solution. The mixture was puton the roller to form the polymer solution. After the clear polymersolution was formed, the required amounts of finely divided conductivepowder (for example, active carbon, carbon black and copper powder) wereslowly added to the polymer solution.

Detailed procedure for the preparation of the first spinning dope whichforms a first (inside) layer in the fibre:

-   -   1. Weighed 100 gram of NMP, and poured it into a 250 ml        wide-neck bottle.    -   2. Weighed 20 gram of PESF, and then added it slowly to the        solvent.    -   3. Put the mixture on a rotary pump to form the polymer        solution. Allow 2-3 days to dissolve the PESF,    -   4. After the clear polymer solution was formed, the bottle was        reset in an IKA® WERKE stirrer at a speed between 500-1000 rpm.    -   5. Weighed 80 gram of 13X adsorbent, and then added it slowly        into the polymer solution. Allow 1-2 days to ensure that the        adsorbent powder dispersed uniformly in the polymer solution.    -   6. The mixture was put back on a rotary pump to degas and form        the uniformly spinning dope. Allow 4-7 days in order to form a        uniform spinning dope.

Detailed procedure for the preparation of second spinning dope whichforms a second (intermediate) layer in the fibre:

-   -   1. Weighed 80 gram of NMP, and poured it into a 250 ml wide-neck        bottle.    -   2. Weighed 20 gram of PESF, and then added it slowly to the        solvent.    -   3. Put the mixture on a rotary pump to form the polymer        solution. Allow 2-3 days to dissolve the PESF.    -   4. After the clear polymer solution was formed, the bottle was        reset in an IKA® WERKE stirrer at a speed between 500-1000 rpm.    -   5. Weighed 80 gram of 4A adsorbent, and then added it slowly        into the polymer solution. Allow 1-2 days to ensure that the        adsorbent powder dispersed uniformly in the polymer solution.    -   6. The mixture was put back on a rotary pump to degas and form        the uniformly spinning dope. Allow 4-7 days in order to form a        uniform spinning dope.

Detailed procedure for preparation of conducting spinning dope (outerlayer) of the fibre:

-   -   1. Weighed 160 gram of NMP and poured it into a 250 ml wide-neck        bottle.    -   2. Weighed 1 gram of polyaniline, and then added it slowly to        the solvent.    -   3. Put the mixture on a rotary pump to form the polymer        solution. Allow 1 day to dissolve the polyaniline.    -   4. The mixture was filtered through the 100 μm Nylon        filter-paper in order to remove the non-dissolved polyaniline.    -   5. Weighed 39 gram of PESF, and then added it slowly to the        solvent.    -   6. Put the mixture on a rotary pump to form the polymer        solution. Allow 2-3 days to dissolve the PESF.    -   7. After the clear polymer solution was formed, the bottle was        reset in an IKA® WERKE stirrer at a speed between 500-1000 rpm.    -   8. Weigh 10 gram of carbon black, and then add it slowly into        the polymer solution. Allow 1 day to ensure that the carbon        powder dispersed uniformly in the polymer solution.    -   9. Weigh 10 gram of active carbon, and then add it slowly into        the polymer solution. Allow 1 day to ensure that the carbon        powder dispersed uniformly in the polymer solution.    -   10. Weigh 10 gram of copper, and then add it slowly into the        polymer solution. Allow 1 day to ensure that the carbon powder        dispersed uniformly in the polymer solution.    -   11. The mixture was put back on a rotary pump to degas and form        the uniformly spinning dope. Allow 4-7 days in order to form a        uniform spinning dope.

The tables below gives spinning conditions for use in the spinnerettefor the preparation of the triple layer hollow fibre using the threespinning dopes described above. The table also summarises the precursormixtures compositions of three layer fibres

TABLE 1 Resistance Ω/(25 cm × Sample Polymer/Solvent Polymer/additivesPressure 100-300 name Wt % Wt % Supply Parameter fibres) Ex. 1 PESF/NMPPESF/13X 2 bar Boreliquid: 4 ml/min 90-15 Internal- 16/84 19/81 Air gap:5 cm layer Roller mixture: 25 rpm Ex. 1 PESF/NMP PESF/4A 1.5 bar   Waterbath: 25° C. Medium- 20/80 20/80 layer Ex. 1 Polyaniline + PESF/Polyaniline + PESF/ 1 bar External- NMP carbon layer 0.5 + 19.5/80black + active carbon + copper 1.4 + 55.7/14.2 + 14.2 + 14.2

TABLE 2 Resistance Ω/(25 cm × Sample Polymer/Solvent Polymer/additivesPressure 100-300 name Wt % Wt % supply Parameter fibres) Ex. 2 PESF/NMPPESF/13X 2 bar Bore 100-25 Internal- 20/80 23.8/72.2 liquid: 4 ml/minlayer Air gap: 5 cm Ex. 2 PESF/NMP PESF/4A 1.5 bar   Roller: 25 rpmMedium- 20/80 29.1/71.9 Water layer bath: Ex. 2 Polyaniline + PESF/NMPPESF/activated 1 bar 25° C. External- 0.4 + 19.6/80 charcoal + carbonlayer black + copper 38/19 + 14.5 + 28.5

Spinning Multi-Layer Conducting Adsorbent Hollow Fibres

The mixtures were transferred to three stainless steel vessels anddegassed by vacuum pump for 1 hour at room temperature before thespinning process. This step was to ensure that the gas bubbles werecompletely removed from the viscous polymer solution. The tank forinternal dope was pressurised to 2-3 bar using nitrogen during thespinning process. The vessel for second layer dope was pressurized to1.5-2 bar using nitrogen during the spinning process. The external layervessel was pressurized to 0.5-1.5 bar keep this pressure below 2ndlayer).

A quadruple orifice spinneret with external layer (d_(out)/d_(in), 4mm/3.2 mm), second layer (d_(out)/d_(in), 2.95 mm/2.25 mm) internallayer (d_(out)/d_(in), 2 mm/1.1 mm), and the bore diameter 0.8 mm wasused to obtain hollow fibre precursors. The air gap was kept at 5-10 cmand water was used as the internal and external coagulator for allspinning runs. Finally, in forming the hollow fibre the precursor waspassed through a water bath to complete the solidification process. Thehollow fibre was then washed thoroughly in a second water bath. It isvery important to ensure that the hollow fibre is not subjected tomechanical dragging throughout the spinning process. Care was taken toensure continuity of the pressure and internal water support in order toavoid entrapment of air and separation of the fibre, which wouldeventually result in an unsuccessful spinning.

The hollow fibre precursors were left to soak for 3-4 days in freshwater; this is being very important to ensure the removal of anyresidual solvent. After the soaking process, the hollow fibre precursorswere dried at ambient conditions for seven days before firing andcharacterization of the inorganic hollow fibre.

FIGS. 1 a and 1 b show the triple layer fibre formed with the SEMs takenat different voltages. The inner (core) layer contains 13X as the activeingredient to primarily adsorb CO₂ from a gas stream. The intermediatelayer contains 4A as the active ingredient and is present primarily toremove moisture from the gas stream. The outer layer is the conductinglayer to pass the current through the fibre and provide localisedheating of the two adsorbents in the inner and intermediate layers andthereby to desorb the materials.

FIGS. 2 a, 2 b and 2 c show each of the three layers at much highermagnification to show in more detail the structure of each layer. FIG. 2a shows the outer conducting layer which is dominated by the carbon andother conducting components. This has a dense structure to enable thecurrent to pass through the fibre but must still have sufficientporosity to allow the gases to pass through to the active intermediateand inner layers. FIG. 2 b shows the intermediate layer which includesthe 4A zeolite and FIG. 2 c shows the inner layer including the 13Xzeolite.

In one embodiment, a bundle of fibres may be grouped together as shown,for example, in FIG. 3. In this case, the end of the bundle of fibresmay be coated with an electrically conductive paste such as silver. Thisis shown more clearly in FIGS. 3 b and 3 c. This simplifies theelectrical supply to the fibre by ensuring that it is not necessary tohave separate supplies to each fibre but a single connection at eachend. It is not essential to have an end cap of silver or carbon and thecurrent could alternatively be supplied to the fibre by means of a wirewrapped round the perimeter of the bundle of fibres which would then beconducted by the conductor (carbon, carbon composite or semi-conductormaterial) in the outer layer.

FIG. 4 shows the heating performance of a triple layer fibre(composition as set out in table 2 above) with different power inputsranging from 20V AC to 50V AC. These results show the fibre heatingwhile the fibre is reaching steady state or optimisation. It has beenfound that the fibres typically reach a steady state and optimisedperformance airier approximately 10 heating and cooling cycles.Referring to FIG. 4, as would be expected the higher the appliedvoltage, the higher the temperature reached. The heating rates of allfour experiments is high and operating temperatures may be reachedquickly. Some zeolites may desorb the adsorbed gases at temperatures aslow as 60-80° C. but typically the temperature should be above 90° C.for desorption. As can clearly be seen from FIG. 4, at the applicationof both 40V and 50V, the temperature of the fibre exceeds 90° C.substantially within 10 minutes.

FIG. 5 shows the heating and cooling performance of a bundle of 100fibres (composition from table 2 above). The applied voltage in eachcase is 40V AC and the resistance of the bundle is 100Ω. The net effectis a voltage range of 10 to 20V. As will be seen from the closeconcordance of the three sets of results, the fibres had substantiallyreached their steady state. Again, the fibres heat up to above 90° C.very quickly (less than 5 minutes) and on the removal of the appliedvoltage at 120 minutes the temperature drops back to close to ambienttemperatures in about 10 minutes. These heating and cooling curves aresubstantially steeper than would be achieved for fibres using theheating techniques of the prior art (oven or flat plates).

FIG. 6 shows the adsorption performance of fibres (composition as setout in table 1 above) once they have reached the equilibrium state. At 0minutes the test gas starts passing through the fibres. For curve (a)the test gas comprises 3000 ppm CO₂ at 1 litre/min with 55% relativehumidity. For curve (b) the gas is similar but without the humidity. Thefibres had been regenerated at 180° C. by application of 35V AC. The CO₂is completely adsorbed by the fibres for just about 2 hours from thestart of the gas flow. After this time, adsorption efficiency decreasesand CO₂ starts to appear in the exit gas. This is called thebreakthrough point and is a first indication that the fibres need to beregenerated.

For the wet gas, the first appearance of CO₂ in the exit gas takesplaces at about 140 minutes and there is then a very rapid increase inthe concentration of the CO₂ in the exit gas peaking at just under 4000ppm after just under 1 hour. The slope of the breakthrough curve is anindication of the efficiency of mass transfer within the system, asharper curve indicates a more efficient system with lower resistance toadsorption and subsequent desorption in regeneration. The moisturepresence in the fibre matrix seems to be improving the CO₂ adsorptionand solubility in the matrix. Moisture adsorption with 4A zeolite fibresbreakthrough times are greater than 2 hours. The internal layer of 13Xand the intermediate layer of 4A both adsorb CO₂, however the kineticadsorption of CO₂ onto 4A is slower and hence the curves for adsorptionon 4A would be shallower and the capacity for CO₂ would be less. Thisshows that two or three types of adsorbents could be incorporated intothe fibre structure either as a mixed matrix or as a layered system toadsorb selected components at different rates. It also shows thebenefits of an open structure with open pore macrovoids proving moreefficient for both adsorption and desorption.

FIG. 7 shows the electrical regeneration performance of the fibres(again, composition from example 1) and in particular the desorption ofCO₂ from the adsorbent. In runs (a) and (b) the fibre was purged with aflow of nitrogen as the electrical current is applied. In both cases thecurrent was 35V AC and for run (a) the purge was 200 ml/min of nitrogenand for run (b) the purge was 100 ml/min of nitrogen. In both cases itcan be seen that the adsorbent is purged of substantially all of theadsorbed CO₂ within 10 minutes. For run (a) the desorption is marginallyquicker with the higher concentration of nitrogen purge.

Double Layer Fibres

The fibres were prepared in similar ways to that set out above with atriple orifice spinnerette being used to produce the double layer fibre.The inner layer includes the active component, in this case 13X which issensitive to the presence of CO2. The composition of the double layerfibre of this example is set out in table 3 below.

TABLE 3 double layer fibre Resistance in the external layerPolymer/solvent Polymer/adsorbent Ω/(25 cm × 100-300 wt (%) wt (%)Fibres) Internal PESF/NMP PESF/13X 120-30 layer 20/80 22/78 ExternalPESF + polyanille/ PESF/activated layer NMP charcoal + carbon 19.8 +0.2/80 black + copper 38/19 + 14.5 + 28.5

FIG. 8 shows an SEM of the double layer fibre formed. The inner layercontains 13X as the active ingredient to primarily adsorb CO2 from a gasstream and the outer layer is the conducting layer to pass the currentthrough the fibre and provide localised heating of the adsorbent in theinner layer and thereby to desorb the material.

FIGS. 9 a and 9 b show each of the layers at much higher magnificationto show in more detail the structure of each layer. FIG. 9 a shows theouter conducting layer which is dominated by the carbon. This again hasa dense structure to enable the current to pass through the fibre butstill has sufficient porosity to allow the gases to pass through to theactive inner layer. FIG. 9 b shows the inner layer which includes the13X zeolite.

In one embodiment, a bundle of fibres such as those shown in FIG. 10 amay be grouped together as shown, for example, in FIG. 10 b. In thiscase, the end of the bundle of fibres may be capped with an electricallyconductive cap with a conductor on the inside which contacts all of thefibres. This simplifies the electrical supply to the bundle of fibres byensuring that it is not necessary to have separate supplies to eachfibre but a single connection at each end of the overall bundle.

FIG. 11 shows the heating performance of a fibre under cyclic heating at40V AC input current. The initial resistance in the fibre was 158Ω butthis decreased down to a steady 118Ω after 6 heating cycles. All of thesubsequent testing was done on fibres which had reached this steadystate with a resistance of 118Ω. The graph also shows that the rate ofheating up increased as the fibre reached steady state and once at thisstate the fibre rapidly increased temperature to 190° C. (withoutinsulation) within 15 minutes and stayed at this level while the voltageremained on.

FIG. 12 shows the steady state heating and cooling performance of doublelayer fibres without the use of a purge during the regeneration step.Again it can be seen that the fibres rapidly heat to a temperature of190° C. (within 20 minutes) and that this is maintained while thevoltage is applied. The voltage is switched off at 120 minutes and it anbe seen that the temperature drops away equally rapidly back downtowards ambient temperatures. Much more rapid heating to 190° C. wasobserved with tripling the fibre numbers (within 5 minutes). The fibresare back at worn temperature within 20 minutes of the voltage beingstopped even without the use of a purge. With a purge the increase anddecrease in temperature may be slightly quicker as the temperaturegradient is maintained by the effective removal of desorbed gas.

FIG. 13 shows the adsorption performance of a number of fibres afterthey have already been regenerated and have reached the steady state.The regeneration took place at 190° C. as described above. For curve (a)the regeneration took place in the presence of a purge of 200 ml/min ofnitrogen. For run (b) the regeneration took place with a lower purge ofjust 100 ml/min of nitrogen. For run (c) the regeneration took place inthe absence of a nitrogen purge but under a low atmospheric vacuum.

FIG. 14 shows the desorption performance of the fibres under a nitrogenpurge (200 ml for curve (a) and 100 ml for curve (b)) at 180° C. asgenerated by an applied voltage of 40V AC. While the use purges is knownin existing techniques for regeneration, the quantity of nitrogenrequired is of the order of 10 times as much as may be used in thepresent invention. However, as indicated above the use of a nitrogen orother gas (e.g. air) purge is not essential in the present inventionwhich works effectively with no purge.

Referring to FIGS. 13 and 14, it can be seen that adsorption of thecarbon dioxide can be achieved rapidly with all fibres and they allprovide a sharper breakthrough curve and much better kinetic adsorptionperformance than existing adsorbents. This results in reduced bed sizesand inventory. Electrical heating under a low vacuum (ETVS) gave animproved performance when compared to the fibres which had beenregenerated with the nitrogen purge. The electrically desorbed CO₂ willbe taken away by the small purge gas flow rate while the vacuum willassist in removing any trapped molecules within the structure. Animproved adsorption capacity is therefore shown by reference to FIG. 14.This shows that complete desorption can be achieved within around 20minutes by electrical heating at 90° C. with a nitrogen purge.

EXAMPLE 4

A double layer fibre made according to the composition set out in table4 below was made. The fibre was heated to 200° C. and was then allowedto cool with different cooling patterns. (a) Fibre module wasregenerated at 200° C. with 200 ml/N₂ purging. (b) Fibre moduleregenerated at 200° C. while vacuuming for 2 hrs without N₂ purging andthen cooling for 1 hr. (c) Fibre module regenerated at 200° C. whilevacuuming for 1 hrs without N₂ purging and then cooling for 4 hrs. (d)Fibre module was regenerated at 200° C. while vacuuming for 1 hrswithout N₂ purging and then cooling for 1 hrs. (e) Fibre module wasregenerated at 200° C. while vacuuming for 30 mins without N₂ purgingand then cooling for 1 hrs. (f) Fibre module was regenerated 200° C.while vacuuming for 20 mins without N₂ purging and then cooling for 1hrs.

TABLE 4 Resistance in the external layer Polymer/solventPolymer/adsorbent Ω/(25 cm × 100-200 wt (%) wt (%) Fibres) InternalPESF/NMP PESF/13X 100-60 layer 20/80 10/90 External PESF + polyanille/PESF/activated layer NMP charcoal + carbon 19.8 + 0.2/80 black + copper38/19 + 15 + 28

FIG. 15 shows the adsorption performance of the double layer fibre andthe different cycles of thermal and vacuum cycling. It is apparent thatadsorbent fibre regeneration can be successfully achieved with vacuumwhile electrically heating at 200° C., for 20-30 minutes without anypurge flow. Further, the adsorption performance of the fibre moduleafter vacuum-thermal regeneration is similar to thermal regenerationWith heated N (for an extended period of time). The breakthrough time issimilar even if heated at a slightly higher temperature (210° C.). Thereis also no substantial difference between 2 hours vacuum, 20 minutesvacuum or heating at 210° C. or 200° C.

EXAMPLES 5 TO 10

Double layer fibres were made in the same way as for example 4, but withthe compositions for the external layer as set out in table 5 below. Ineach of examples 5 to 10 the internal layer is 20% PESF/80% 13Xadsorbent by weight. FIG. 16 shows the temperature profile for these 6examples for different applied voltages where the voltage ranging, from20V to 150V AC is applied for 2 minutes. In each case a bundle of 25fibres is heated by application of the voltage.

TABLE 5 The various compositions of fibre conductive layer (externallayer) Polymer/solvent Polymer/adsorbent resistance Dope No Wt (%) Wt(%) additives Ω/cm Example 5 PESF + polyaniline/ PESF/activated none 80NMP 15 + 0.5/84.5 charcoal 27.9/72.1 Example 6 PESF/NMP PESF/activatedPolyaniline 193 15.3/84.7 charcoal composite 33/67 20 wt % in carbon 2 gExample 7 PESF/NMP PESF/activated Polypyrrole 196 15.3/84.7 charcoalcomposite 33/67 20 wt % in carbon 2 g Example 8 PESF + polyaniline/PESF/activated none 60 NMP 19.8 + 0.2/80 charcoal + carbon black50/31.25 + 18.75 Example 9 PESF + polyaniline/ PESF/activated none 90NMP 19.8 + 0.2/80 charcoal + carbon black + 4A 35.3/20.6 + 14.7 + 29.4Example 10 PESF + polyaniline/ PESF/semi- none 120 NMP 19.8 + 0.2/80conducting material 25/75

Referring to table 5 and FIG. 16, it can be seen that a range ofproperties are available by varying and controlling the resistance andconductivity properties of the fibre layer. This is largely determinedby the selection of polymer/solvent and the presence or absence of anadditive/conducting materials. The appropriate use of such additives andthe thickness of the conducting layer can closely control the resistanceand hence the voltage and the required regeneration temperature of thefibre.

For the multilayer fibres prepared using composition set out in anexample 5 very high temperatures could be reached with a very shortspace of time, in excess of 300° C. in 2 minutes of heating at anapplied, voltage of about 108V AC. The conductivity of the hollow fibreprepared from (PESF+polyaniline) and activated charcoal with carbonblack (Example 8) gives a lower resistance (60 ohm/cm) and goodconductivity. It is possible to achieve regenerable temperatures usinglow voltages. When the voltage applied was up to 50VAC the temperatureof hollow fibre reached at 190° C. in 2 minutes.

1-31. (canceled)
 32. A multi-layer hollow fibre comprising: an internallayer comprising an organic polymer; and an inorganic adsorbent; anexternal layer comprising an electrically conductive component.
 33. Thehollow fibre of claim 32, wherein the organic polymer is selected fromthe group consisting of PESF, polysulfone, polyvinylidenefluoride(PVDF), polyethylene, polypropylene, poly(phenylene oxide),polymethylmethacrylate, poly(vinyl chloride), Polysulfone, Poly(ethersulfone), Poly(vinylidene fluoride), Polyacrylonitrile, Celluloseacetate, Polymide Poly(ether imide), Polyamide (aromatic), Polyimide,Poly(ether imide) and poly(vinyl alcohol) co-polymers of Polylactide(PLA) and Polyglycolide (PGA), Polycaprolactone (PCL) and Poly(ethyleneterephathalate) (PET).
 34. The hollow fibre of claim 32, wherein theadsorbent is selected from silicalite ZSM5, MCM41, MCM48, a silicaadsorbent, an activated carbon powder, an ion exchange resin, and acombination of two or mere thereof.
 35. The hollow fibre of claim 32,wherein the electrically conductive component is selected from the groupconsisting of silver, a metal powder, carbon, a conducting polymer,conducting cement, a semiconductor material, and a combination of two ormore thereof.
 36. The hollow fibre of claim 32, wherein the fibre has aflexibility of greater than 5° bending angle from the midpoint of thefibre.
 37. The hollow fibre of claim 35, wherein the electricallyconductive component comprises a conductive polymer.
 38. The hollowfibre of claim 37, wherein the electrically conductive component furthercomprises a conductive powder.
 39. The hollow fibre of claim 38, whereinthe conductive powder is selected from active carbon, carbon black,copper powder, and a combination of two or more thereof.
 40. The hollowfibre of claim 32, wherein the outer diameter of the fibre is from 400microns to 2.5 cm.
 41. The hollow fibre of claim 32, wherein the fibrehas a mechanical strength of greater than 200 g force at a crossheadspeed of 1.0 mm/sec for a fibre with an effective surface porosity(ε/q²) of 0.1-0.2, as calculated from Knudsen flow method.
 42. Thehollow fibre of claim 32, wherein the fibre has an area to volume ratiogreater than 1000 m²/m³.
 43. The hollow fibre of claim 32, wherein theinorganic adsorbent is a zeolite.
 44. The fibre of claim 32, wherein theexternal layer further comprises an additive selected from polyvinylalcohol, polyvinyl pyrrolidone, polyacrylic acid, calcium chloride,fumed silica and a combination of two or more thereof.
 45. The fibre ofclaim 32, wherein the fibre is substantially defect free.
 46. The fibreof claim 32, wherein the fibre has a graded pore structure.
 47. A gasadsorption unit comprising a plurality of fibred according to claim 32.48. The gas adsorption unit of claim 47, wherein the plurality of fibresare grouped together in a bundle.
 49. The gas adsorption unit of claim48, wherein the bundle of fibres is coated with an electricallyconductive paste.
 50. The gas adsorption unit of claim 49, furthercomprising a wire wrapped around the bundle of fibres.
 51. The gasadsorption unit of claim 47, further comprising a housing.